Get the free IRB Modification Request Form. A. Study Information IRB Study # - depts washington
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IRB #: 13744 Study Title: Managing Childhood Abdominal Pain (MAP) Principal Researcher: RNA Levy, PhD Revision Date: 07/07/11 Protocol Version: 1 ASSENT FORM For Participants 712 Years of Age 41213
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How to fill out irb modification request form
How to Fill Out IRB Modification Request Form:
01
Start by downloading the IRB Modification Request Form from the official website or obtaining a physical copy from the IRB office.
02
Ensure that you have all the necessary information and supporting documentation before you begin filling out the form. This may include research protocols, consent forms, participant recruitment materials, or any other relevant documents.
03
Begin by providing your personal information in the designated fields, such as your name, contact information, and institutional affiliation.
04
State the title of your research project and provide a brief summary of the proposed modifications you wish to make to the approved protocol.
05
Clearly articulate the specific changes you want to implement, explaining why they are necessary and how they will impact the study. Be as detailed and precise as possible to facilitate a thorough review by the IRB committee.
06
If applicable, include any revised consent forms or other participant-facing materials that need to be reviewed and approved along with the modifications.
07
Provide any supporting documentation that may be required, such as updated literature reviews, additional research findings, or relevant certifications.
08
Sign and date the form, and make sure to keep a copy for your records before submitting it to the IRB office.
Who Needs an IRB Modification Request Form:
01
Researchers who have already obtained IRB approval for their study but need to make changes to the approved protocol.
02
Individuals conducting research involving human subjects at institutions that require IRB oversight and approval.
03
Researchers who want to modify the study design, recruit different participants, alter data collection methods, or make any other substantive changes that could potentially affect the ethical considerations of the study.
Remember, it is essential to consult with your institutional IRB office or review board for specific guidelines and requirements when it comes to filling out the IRB Modification Request Form.
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What is irb modification request form?
The IRB modification request form is a document used to request changes to an approved research study.
Who is required to file irb modification request form?
Researchers conducting human subjects research are required to file an IRB modification request form.
How to fill out irb modification request form?
To fill out an IRB modification request form, researchers must provide details about the proposed changes to the study protocol.
What is the purpose of irb modification request form?
The purpose of the IRB modification request form is to ensure that any changes to the study protocol are reviewed and approved by the IRB before implementation.
What information must be reported on irb modification request form?
The IRB modification request form must include details about the proposed changes, rationale for the changes, and any potential risks to study participants.
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